ENST00000389048.8:c.3794T>G
MANE Select
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ENSP00000373700.3:p.Val1265Gly
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ENST00000431873.6:c.1021T>G
|
|
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ENST00000638605.1:n.671T>G
|
|
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ENST00000642122.1:c.590T>G
|
ENSP00000493203.1:p.Val197Gly
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ENST00000389048.7:c.3794T>G
|
ENSP00000373700.3:p.Val1265Gly
|
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ENST00000431873.5:c.674T>G
|
ENSP00000414027.2:p.Val225Gly
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ENST00000618119.4:c.2663T>G
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ENSP00000482733.1:p.Val888Gly
|
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NM_004304.4:c.3794T>G
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NP_004295.2:p.Val1265Gly
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NM_001353765.1:c.590T>G
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NP_001340694.1:p.Val197Gly
|
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XM_024452778.1:c.947T>G
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XP_024308546.1:p.Val316Gly
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XM_024452779.1:c.590T>G
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XP_024308547.1:p.Val197Gly
|
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NM_004304.5:c.3794T>G
MANE Select
|
NP_004295.2:p.Val1265Gly
|
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NM_001353765.2:c.590T>G
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NP_001340694.1:p.Val197Gly
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